Human IgG Subclasses against Enterovirus Type 71: Neutralization versus Antibody Dependent Enhancement of Infection

The emerging human enterovirus 71 (EV71) represents a growing threat to public health, and no vaccine or specific antiviral is currently available. Human intravenous immunoglobulin (IVIG) is clinical used in treating severe EV71 infections. However, the discovery of antibody dependent enhancement (A...

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Published inPloS one Vol. 8; no. 5; p. e64024
Main Authors Cao, Rui-Yuan, Dong, Da-Yong, Liu, Rui-Ju, Han, Jian-Feng, Wang, Guang-Chuan, Zhao, Hui, Li, Xiao-Feng, Deng, Yong-Qiang, Zhu, Shun-Ya, Wang, Xiao-Yu, Lin, Fang, Zhang, Fu-Jun, Chen, Wei, Qin, E-De, Qin, Cheng-Feng
Format Journal Article
LanguageEnglish
Published United States Public Library of Science 20.05.2013
Public Library of Science (PLoS)
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Summary:The emerging human enterovirus 71 (EV71) represents a growing threat to public health, and no vaccine or specific antiviral is currently available. Human intravenous immunoglobulin (IVIG) is clinical used in treating severe EV71 infections. However, the discovery of antibody dependent enhancement (ADE) of EV71 infection illustrates the complex roles of antibody in controlling EV71 infection. In this study, to identify the distinct role of each IgG subclass on neutralization and enhancement of EV71 infection, different lots of pharmaceutical IVIG preparations manufactured from Chinese donors were used for IgG subclass fractionation by pH gradient elution with the protein A-conjugated affinity column. The neutralization and ADE capacities on EV71 infection of each purified IgG subclass were then assayed, respectively. The neutralizing activity of human IVIG is mainly mediated by IgG1 subclass and to less extent by IgG2 subclass. Interestingly, IgG3 fraction did not have neutralizing activity but enhanced EV71 infection in vitro. These results revealed the different roles of human IgG subclasses on EV71 infection, which is of critical importance for the rational design of immunotherapy and vaccines against severe EV71 diseases.
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Current address: Institute of Biotechnology, Academy of Military Medical Sciences, Beijing, China
Conceived and designed the experiments: CFQ RYC. Performed the experiments: RYC DYD FJZ JFH GCW HZ. Analyzed the data: RYC WC EDQ CFQ. Contributed reagents/materials/analysis tools: XFL YQD SYZ XYW FL RJL. Wrote the paper: RYC CFQ.
Competing Interests: Commercial IVIG products are kindly provided by Tonrol and Ronsen Pharmaceuticals, and this does not alter the authors’ adherence to all the PLOS ONE policies on sharing data and materials.
ISSN:1932-6203
1932-6203
DOI:10.1371/journal.pone.0064024